State Key Laboratory of Emerging Infectious Diseases and Department of Microbiology, The University of Hong Kong, Pokfulam, Hong Kong.
School of Biomedical Sciences, The University of Hong Kong, Pokfulam, Hong Kong.
Emerg Microbes Infect. 2021 Dec;10(1):291-304. doi: 10.1080/22221751.2021.1885998.
Effective treatments for coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) are urgently needed. Dexamethasone has been shown to confer survival benefits to certain groups of hospitalized patients, but whether glucocorticoids such as dexamethasone and methylprednisolone should be used together with antivirals to prevent a boost of SARS-CoV-2 replication remains to be determined. Here, we show the beneficial effect of methylprednisolone alone and in combination with remdesivir in the hamster model of SARS-CoV-2 infection. Treatment with methylprednisolone boosted RNA replication of SARS-CoV-2 but suppressed viral induction of proinflammatory cytokines in human monocyte-derived macrophages. Although methylprednisolone monotherapy alleviated body weight loss as well as nasal and pulmonary inflammation, viral loads increased and antibody response against the receptor-binding domain of spike protein attenuated. In contrast, a combination of methylprednisolone with remdesivir not only prevented body weight loss and inflammation, but also dampened viral protein expression and viral loads. In addition, the suppressive effect of methylprednisolone on antibody response was alleviated in the presence of remdesivir. Thus, combinational anti-inflammatory and antiviral therapy might be an effective, safer and more versatile treatment option for COVID-19. These data support testing of the efficacy of a combination of methylprednisolone and remdesivir for the treatment of COVID-19 in randomized controlled clinical trials.
急需有效治疗由严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 引起的 2019 年冠状病毒病 (COVID-19)。地塞米松已被证明能使某些住院患者获益,但糖皮质激素如地塞米松和甲泼尼龙是否应与抗病毒药物联合使用以防止 SARS-CoV-2 复制增加仍有待确定。在这里,我们展示了甲泼尼龙单独使用和与瑞德西韦联合使用在 SARS-CoV-2 感染的仓鼠模型中的有益效果。甲泼尼龙治疗可增强 SARS-CoV-2 的 RNA 复制,但可抑制病毒诱导的人单核细胞衍生巨噬细胞中促炎细胞因子的产生。虽然甲泼尼龙单药治疗可缓解体重减轻以及鼻和肺炎症,但病毒载量增加,针对刺突蛋白受体结合域的抗体反应减弱。相比之下,甲泼尼龙与瑞德西韦联合治疗不仅可防止体重减轻和炎症,还可抑制病毒蛋白表达和病毒载量。此外,在存在瑞德西韦的情况下,甲泼尼龙对抗体反应的抑制作用减轻。因此,联合抗炎和抗病毒治疗可能是 COVID-19 的一种有效、更安全、更通用的治疗选择。这些数据支持在随机对照临床试验中测试甲泼尼龙和瑞德西韦联合治疗 COVID-19 的疗效。